在不同ECMO模式下,聚米辛B的药理动力学变化和影响因素
Mi Xu1, Na Chen2, Yong-Wei Yu1
1Department of Critical Care Medicine, The First Affiliated Hospital of Zhejiang University School of Medicine, Hangzhou, Zhejiang, People's Republic of China.
Infection and drug resistance
|December 30, 2024
概括
研究了在体外膜氧化 (ECMO) 期间的多素B水平. ECMO流量和持续的替代疗法影响了Polymyxin B的药理动力学,影响了细菌清除.
科学领域:
- 药理动力学 药理动力学
- 传染性疾病 传染性疾病
- 关键护理医学 关键护理医学
背景情况:
- 身体外膜氧化 (ECMO) 支持的持续时间增加,增加了细菌耐药性的风险.
- 聚米辛B (PMB) 治疗耐药性感染,但其药理动力学 (PK) 可以在ECMO期间发生变化,冒着错误剂量的风险.
- 在ECMO期间了解PMB PK对于有效治疗耐药细菌感染至关重要.
研究的目的:
- 为了研究在ECMO过程中波利米辛B (PMB) 药动力学参数的变化.
- 为了确定影响PMB水平的因素,在静脉或静脉动脉ECMO患者.
- 为了将PMB度与ECMO患者的细菌清除相关联.
主要方法:
- 一项前性药理动力学研究,涉及11名ECMO患者的耐药细菌.
- 在稳定状态下,在氧化器前后测量PMB度.
- 使用非线性混合效应建模和分析微生物培养结果,开发一个人群PK模型.
主要成果:
- 在氧化器之前和之后的PMB度没有显著差异.
- 一个两部分的模型描述了PMB PK,ECMO流量影响清除 (CL) 和CRRT影响中央体积.
- 较高的平均稳定状态度 (Css,avg) 与成功的细菌清除相关.
结论:
- 在ECMO氧化器中,PMB度稳定.
- 持续置换疗法 (CRRT) 可能会改变ECMO患者的PMB药理学.
- 建议对PMB进行治疗药物监测,以优化ECMO患者的临床结果.
相关概念视频
Factors Affecting Dissolution: Polymorphism, Amorphism and Pseudopolymorphism
231
Polymorphism refers to the existence of a drug substance in multiple crystalline forms, known as polymorphs. Recently, this term has been expanded to include solvates (forms containing a solvent), amorphous forms (non-crystalline forms), and desolvated solvates (forms from which the solvent has been removed).
Some polymorphic crystals possess lower aqueous solubility than their amorphous counterparts, leading to incomplete absorption. For instance, the oral suspension of Chloramphenicol, which...
Some polymorphic crystals possess lower aqueous solubility than their amorphous counterparts, leading to incomplete absorption. For instance, the oral suspension of Chloramphenicol, which...
231
Chronopharmacokinetics: Circadian Rhythms and Influence on Drug Response
31
Circadian rhythms are cyclic changes that are crucial in plasma drug concentrations. Various standard circadian parameters, including core body temperature, heart rate, and other cardiovascular factors, directly impact disease states and the therapeutic response to drug therapy.
The time of drug administration is an important factor to consider, as it can influence the toxic dose of a drug. For example, a study conducted by Prins et al. in 1997 examined the effects of the timing of...
The time of drug administration is an important factor to consider, as it can influence the toxic dose of a drug. For example, a study conducted by Prins et al. in 1997 examined the effects of the timing of...
31
Factors Affecting Drug Biotransformation: Biological
68
Biological factors significantly impact drug metabolism, influencing drug clearance, efficacy, and potential toxicity.
Species differences: Variations in enzyme systems across species can cause disparities in drug metabolism. For instance, humans may metabolize certain drugs faster than rodents, altering therapeutic effects.
Strain differences: Genetic variations within a species can result in differing enzyme activity, impacting drug response and toxicity. For example, some mouse strains may...
Species differences: Variations in enzyme systems across species can cause disparities in drug metabolism. For instance, humans may metabolize certain drugs faster than rodents, altering therapeutic effects.
Strain differences: Genetic variations within a species can result in differing enzyme activity, impacting drug response and toxicity. For example, some mouse strains may...
68
Factors Affecting Renal Clearance: Drug Distribution and Drug Interactions
55
Renal clearance plays a pivotal role in drug elimination from the body and can be influenced by drug distribution and interactions. Understanding these factors is crucial in pharmacology as they impact the effectiveness and duration of drug therapy.
One important factor is the relationship between renal clearance and the apparent volume of distribution. Renal clearance tends to be inversely proportional to the apparent volume of distribution. Drugs with an extensive distribution volume or those...
One important factor is the relationship between renal clearance and the apparent volume of distribution. Renal clearance tends to be inversely proportional to the apparent volume of distribution. Drugs with an extensive distribution volume or those...
55
Two-Compartment Open Model: Extravascular Administration
105
The two-compartment model for extravascular administration represents a drug's absorption and distribution process. It features a central compartment, where the drug is first absorbed, and a peripheral compartment, which illustrates the drug's distribution throughout the body. The rate of change in drug concentration in the central compartment is calculated by three exponents: absorption, distribution, and elimination.
The absorption exponent (ka) indicates the speed at which the drug...
The absorption exponent (ka) indicates the speed at which the drug...
105
Factors Affecting Renal Clearance: Drug's Physicochemical Properties and Plasma Levels
113
Renal clearance of a drug is influenced by various factors, including its physicochemical properties and plasma levels. These factors play a significant role in determining how efficiently the kidneys eliminate a drug.
One important factor is the drug's molecular size. The kidneys readily excrete smaller molecules below 300 Daltons (Da). On the other hand, molecules weighing between 300 and 500 Da are excreted through both urine and bile. Larger molecules above 500 Da tend to be excreted...
One important factor is the drug's molecular size. The kidneys readily excrete smaller molecules below 300 Daltons (Da). On the other hand, molecules weighing between 300 and 500 Da are excreted through both urine and bile. Larger molecules above 500 Da tend to be excreted...
113


